37592-72-6

Basic information

• Product Name: 4'-N-HEXYLACETOPHENONE
• Synonyms: TIMTEC-BB SBB008299;P-HEXYLACETOPHENONE;1-(4-hexylphenyl)-ethanon;Ethanone, 1-(4-hexylphenyl)-;LABOTEST-BB LT00159052;4'-HEXYLACETOPHENONE;4'-N-HEXYLACETOPHENONE;4-N-HEXYLACETOPHENONE
• CAS NO: 37592-72-6
• Molecular Formula: C₁₄H₂₀O
• Molecular Weight: 204.31
• Product Categories: Acetophenones (Building Blocks for Liquid Crystals);Building Blocks for Liquid Crystals;Functional Materials
• Mol File: 37592-72-6.mol
• Article Data: 23

Chemical Properties

• Boiling Point: 132-135°C 2mm
• Flash Point: 132-135°C/2mm
• Appearance: /
• Density: 0,94 g/cm3
• Vapor Pressure: 0.000668mmHg at 25°C
• Refractive Index: 1.5140
• Storage Temp.: Sealed in dry,Room Temperature
• BRN: 1942064
• CAS DataBase Reference: 4'-N-HEXYLACETOPHENONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-N-HEXYLACETOPHENONE(37592-72-6)
• EPA Substance Registry System: 4'-N-HEXYLACETOPHENONE(37592-72-6)

Safety Data

• Safety Statements: 24/25
• TSCA: Yes
• Hazardous Substances Data: 37592-72-6(Hazardous Substances Data)

Usage

General Description

4'-N-HEXYLACETOPHENONE is an organic chemical compound with the chemical formula C14H18O. It is also known by the name 4-acetylphenyl n-hexyl ketone. It is a clear, colorless liquid with a faint, sweet, floral odor. 4'-N-HEXYLACETOPHENONE is commonly used as a flavoring agent and fragrance ingredient in the production of perfumes, soaps, and cosmetics. It is also used as an intermediate in the manufacturing of pharmaceuticals and other chemicals. 4'-N-HEXYLACETOPHENONE exhibits low toxicity and is considered to be relatively safe for use in consumer products when handled and used according to proper safety guidelines.

InChI:InChI=1/C14H20O/c1-3-4-5-6-7-13-8-10-14(11-9-13)12(2)15/h8-11H,3-7H2,1-2H3

Upstream product

• 928-65-4 hexyltrichlorosilane 
• 21369-64-2 n-hexyllithium 
• 99-90-1 para-bromoacetophenone 
• 13329-40-3 4-Iodoacetophenone 
• 111-25-1 1-bromo-hexane 
• 1626436-23-4 C₆H₁₃I₂In 
• 638-45-9 1-Iodohexane 
• 544-10-5 1-Chlorohexane 
• 109613-00-5 4-acetophenyl triflate 
• 186581-53-3 diazomethane 
• 50606-95-6 4-hexylbenzoyl chloride 
• 16343-08-1 hexylboronic acid 
• 99-91-2 para-chloroacetophenone 
• 1077-16-3 hexylbenzene 

Downstream Products

• 14333-88-1 2-(4-hexylphenyl)-2-oxoacetaldehyde 
• 20330-59-0 N-(4-hexylphenyl)acetamide 
• 64328-69-4 2-bromo-1-(4-hexylphenyl)ethan-1-one 
• 81539-57-3 2-Chloro-1-(4-hexyl-phenyl)-ethanone 
• 100-21-0 terephthalic acid 
• 78575-33-4 (4-Hexyl-phenyl)-[(E)-hydroxyimino]-acetaldehyde oxime 
• 1359983-62-2 C₁₅H₂₁N₃*ClH 
• 1359983-80-4 C₂₀H₂₉N₃O₂ 

Relevant articles and documents

One-step synthesis of novel flavylium salts containing alkyl side chains in their 3-, 4′-, 5- or 6-positions and their photophysical properties in micellar media

A one-step preparation of several flavylium salts containing alkyl side chains in their 3-, 4′-, 5- or 6-positions is described. Flavylium salts with alkyl side chains in positions 3 or 4′ were isolated from reactions between 2,4-dihydroxybenzaldehyde and

Visible-Light-Induced Nickel-Catalyzed Cross-Coupling with Alkylzirconocenes from Unactivated Alkenes

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Cesium carbonate-catalyzed indium insertion into alkyl iodides and their synthetic utilities in cross-coupling reactions

A catalytic amount of cesium carbonate (10?mol%) was found to be capable of effectively catalyzing the insertion of indium powder into alkyl iodides. The thus-generated alkyl indium reagents could readily undergo palladium-catalyzed cross-coupling reactions with a wide variety of aryl halides, showing compatibility to a range of important functional groups.